Evidence map›Paper›PMID 39801466›Full record

ArticleChemMedChem2025

APH Inhibitors that Reverse Aminoglycoside Resistance in Enterococcus casseliflavus.

Elise Kaplan, Laurent Chaloin, Jean-François Guichou, Kévin Berrou, Rahila Rahimova, Gilles Labesse, Corinne Lionne

Abstract read
In one paragraph

Article in ChemMedChem, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

Elise KaplanInstitut de Recherche en Infectiologie de Montpellier - IRIM, University of Montpellier, CNRS UMR 9004, 1919 route de Mende, 34293, Montpellier cedex 5, France.ORCID https://orcid.org/0000-0003-4985-1482
Laurent ChaloinInstitut de Recherche en Infectiologie de Montpellier - IRIM, University of Montpellier, CNRS UMR 9004, 1919 route de Mende, 34293, Montpellier cedex 5, France.ORCID https://orcid.org/0000-0002-5757-5804
Jean-François GuichouCentre de Biologie Structurale - CBS, University of Montpellier, CNRS UMR 5048, INSERM U 1054, 29 rue de Navacelles, 34090, Montpellier, France.ORCID https://orcid.org/0000-0002-7699-3235
Kévin BerrouInstitut de Recherche en Infectiologie de Montpellier - IRIM, University of Montpellier, CNRS UMR 9004, 1919 route de Mende, 34293, Montpellier cedex 5, France.ORCID https://orcid.org/0000-0002-2295-2702
Rahila RahimovaCentre de Biologie Structurale - CBS, University of Montpellier, CNRS UMR 5048, INSERM U 1054, 29 rue de Navacelles, 34090, Montpellier, France.ORCID https://orcid.org/0000-0002-4992-842X
Gilles LabesseCentre de Biologie Structurale - CBS, University of Montpellier, CNRS UMR 5048, INSERM U 1054, 29 rue de Navacelles, 34090, Montpellier, France.ORCID https://orcid.org/0000-0002-6861-3300
Corinne LionneInstitut de Recherche en Infectiologie de Montpellier - IRIM, University of Montpellier, CNRS UMR 9004, 1919 route de Mende, 34293, Montpellier cedex 5, France.ORCID https://orcid.org/0000-0002-6348-5311

Funding

Agence Nationale de la Recherche ANR-19-AMRB-0001
6 · The paper itself

Abstract

Aminoglycoside-phosphotransferases (APHs) are a class of bacterial enzymes that mediate acquired resistance to aminoglycoside antibiotics. Here we report the identification of small molecules counteracting aminoglycoside resistance in Enterococcus casseliflavus. Molecular dynamics simulations were performed to identify an allosteric pocket in three APH enzymes belonging to 3' and 2'' subfamilies in which we then screened, in silico, 12,000 small molecules. From a subset of only 14 high-scored molecules tested in vitro, we identified a compound, named here EK3, able to non-competitively inhibit the APH(2'')-IVa, an enzyme mediating clinical gentamicin resistance. Structure-activity relationship (SAR) exploration of this hit compound allowed us to identify a molecule with improved enzymatic inhibition. By measuring bacterial sensitivity, we found that the three best compounds in this series restored bactericidal activity of various aminoglycosides, including gentamicin, without exhibiting toxicity to HeLa cells. This work not only provides a basis to fight aminoglycoside resistance but also highlights a proof-of-concept for the search of allosteric modulators by using in silico methods.

Indexed as

AminoglycosidesAnti-Bacterial AgentsDrug Resistance, BacterialEnterococcusEnzyme InhibitorsKanamycin KinaseDose-Response Relationship, DrugHeLa CellsHumansMicrobial Sensitivity TestsMolecular Dynamics SimulationMolecular StructurePhosphotransferases (Alcohol Group Acceptor)Structure-Activity Relationshipaminoglycoside 2''-phosphotransferaseAminoglycosidesAnti-Bacterial AgentsEnzyme InhibitorsKanamycin KinasePhosphotransferases (Alcohol Group Acceptor)AllosteryAntibiotic resistanceInhibitorsMolecular dockingVirtual screening

Identifiers

PMID39801466
PMCPMC12005471

What OpenQuestion holds

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LicenceCC BY-NC-ND
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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.